Heterojunction photocatalyst for catalytic reduction of CO2, and preparation of heterojunction photocatalyst
A photocatalyst and heterojunction technology, applied in physical/chemical process catalysts, chemical instruments and methods, chemical/physical processes, etc., can solve problems such as low yield and poor catalytic activity, and achieve reduced recombination rate, CO2 The effect of improved restoring ability and low cost
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Embodiment 1
[0024] g-C 3 N 4 Preparation of powder: Weigh 25g of urea into a glass mortar, grind it hard for 2 hours, transfer it to an alumina crucible, wrap it with aluminum foil and seal it, heat it to 400 degrees at a rate of 16 degrees per minute and then keep it warm for 2 hours , increased to 550°C with the same heating rate and held for another 2 hours. Cool the crucible to room temperature naturally, and grind the obtained light yellow powder, namely g-C 3 N 4 .
[0025] 20wt% Bi 2 o 3 doped g-C 3 N 4 Preparation of heterojunction photocatalyst: Weigh 0.5 g of g-C 3 N 4 , which was dissolved in 60 ml ethylene glycol and sonicated for 30 min to obtain flake g-C 3 N 4 . Subsequently, 0.104 g of Bi(NO 3 ) 3 ·5H 2 O and 1 g of urea, stirred vigorously for 30 min to obtain a homogeneous solution. The solution was hydrothermally treated at 180°C for 12 hours in a Teflon-lined autoclave. The obtained product was washed several times with deionized water and dried at 80-...
Embodiment 2
[0027] Adopt then embodiment 1 identical g-C 3 N 4 The method of preparation differs in that:
[0028] 40wt% Bi 2 o 3 doped g-C 3 N 4 Preparation of heterojunction photocatalyst: Weigh 0.5 g of g-C 3 N 4 , which was dissolved in 60 ml ethylene glycol and sonicated for 30 min to obtain flake g-C 3 N 4 . Subsequently, 0.208 g of Bi(NO 3 ) 3 ·5H 2 O and 1 g of urea, stirred vigorously for 30 min to obtain a homogeneous solution. The solution was hydrothermally treated at 180°C for 12 hours in a Teflon-lined autoclave. The obtained product was washed several times with deionized water and dried at 80-100°C. The hydrothermal product was then calcined in air at 380 °C for 2 hours to finally obtain 40 wt% Bi 2 o 3 doped g-C 3 N 4 heterojunction photocatalysts.
Embodiment 3
[0030] Adopt then embodiment 1 identical g-C 3 N 4 The method of preparation differs in that:
[0031] 60wt% Bi 2 o 3 doped g-C 3 N 4 Preparation of heterojunction photocatalyst: Weigh 0.5 g of g-C 3 N 4 , which was dissolved in 60 ml ethylene glycol and sonicated for 30 min to obtain flake g-C 3 N 4 . Subsequently, 0.312 g of Bi(NO 3 ) 3 ·5H 2O and 1 g of urea, stirred vigorously for 30 min to obtain a homogeneous solution. The solution was hydrothermally treated at 180°C for 12 hours in a Teflon-lined autoclave. The obtained product was washed several times with deionized water and dried at 80-100°C. The hydrothermal product was then calcined in air at 380 °C for 2 hours to finally obtain 60 wt% Bi 2 o 3 Doped g-C 3 N 4 heterojunction photocatalysts.
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